Heidi Moua Mlscm

Heidi Moua MLS(ASCP)cm currently serves as the Principal Regulatory Affairs Specialist at Werfen since April 2024. Prior to this role, Heidi was the In-vitro Diagnostics Lead Auditor at TUV SUD from July 2022 to April 2024, and worked as a Client Manager in the Medical Devices/In-vitro Diagnostics Division at BSI from January 2018 to July 2022. Additional experience includes serving as a Clinical Software Specialist at HemaTerra Technologies and as a Clinical Operations Manager at Confirmatrix Laboratory Inc. Heidi Moua holds a Master's degree in Biopharmaceutical Regulatory Affairs from the University of Georgia and a Bachelor's degree in Biological and Biomedical Sciences from the Medical College of Georgia at Augusta University, along with a degree in Clinical Laboratory Science from the Medical College of Georgia School of Medicine.